Passive safety I.V. blood collection catheter

ABSTRACT

Apparatus and methods for a single, handheld device that provides for both insertion of a catheter and collection of a fluid. Some embodiments further include a needle that assists in the insertion of the catheter into a blood vessel, and which includes a retraction feature that protects the user from an accidental needle stick when the device is ready for disposal. Still further embodiments include a protective cover that prevents a user from accidentally being stuck by a second needle used for the introduction of the patient&#39;s blood into a collection device.

CROSS REFERENCE TO RELATED APPLICATION

This application is a continuation of U.S. patent application Ser. No.14/068,630, filed Oct. 31, 2013, which issued as U.S. Pat. No. 9,456,775on Oct. 4, 2016, and claims the benefit of priority to U.S. ProvisionalPatent Application Ser. No. 61/874,771, filed Sep. 6, 2013, all of whichare incorporated herein by reference.

FIELD OF THE INVENTION

Various embodiments of the present invention pertain to methods andapparatus for injecting medicaments into a patient and also taking ablood sample from a patient, and including embodiments having a needleretractable to within a guarded chamber after usage.

BACKGROUND OF THE INVENTION

Fluid access into the vasculature of a patient may be necessary for anyof several different reasons. Such access may be necessary in order toplace medicaments within the patient's circulatory system, or to removeblood or other fluids from the patient for subsequent analysis. Foreither reason, such access is generally established with the vasculatureof the patient, such as a vein. When an infusion protocol is involvedthat requires periodic injections, an established fluid access site thatcan be repetitively used for a sequence of different injections may berequired. Establishing such an access site, however, can be problematic.

Often, such access is established by a needle extending through thelumen of a catheter, such that both the tip of the needle and the tip ofthe catheter are located within the patient's vein. The needle issubsequently withdrawn, and the infusion or injections occur after areservoir and tubing are attached to the luer of the catheter. In yetother situations, it is desirable to obtain blood or other bodily fluidfrom the patient for subsequent analysis. In such cases the blood may bedrawn through a hollow needle inserted into the patient's vasculature orby connection of a blood collection reservoir to an existing, insertedcatheter.

Currently, these two functions of introduction of a medicament into thepatient, and withdrawal of blood from the patient, are performed in aseries of multiple operations by a medical professional, using aplurality of different devices. The current requirement for multiplesteps in a procedure using multiple devices provides multipleopportunities for error and multiple risks to the patient. Further, theuse of multiple devices requires the clinic administrator to maintain aninventory of many separate devices. Such an inventory is not justexpensive, but by itself leads to further risk to the patient if thewrong devices are stocked or used.

Yet further risks are incurred by the medical practitioner, since thedevices used for introduction of a medicament or withdrawal of patientblood each can include sharp tipped needles. Since these needles areexposed to the patient's blood, there is a possibility of the medicalpractitioner being accidentally stuck by a used needle, with thesubsequent exposure of the practitioner to the ailment of the patient.

What is needed are devices that address one or more of theaforementioned issues. Various embodiments of the present invention dothis in novel and unobvious ways.

SUMMARY OF THE INVENTION

Various aspects of different embodiments of the present inventionpertain to the combination of catheter placement for repeat usage, withpatient fluid collection at the time of initial placement of thecatheter.

Yet other embodiments include aspects directed toward safety featuresthat protect a medical professional from being pierced accidentally bythe needle used to introduce the catheter into the patient's circulatorysystem.

Yet other embodiments include aspects directed toward protection of themedical professional from being accidentally pierced with a needle usedto place the patient's blood within a collection vial.

One aspect of the present invention pertains to an apparatus forcollecting blood in a container and connecting to intravenous tubing.Some embodiments include a main body including a collection cavityadapted and configured to receive therein an end of a separatecontainer. Other embodiments include a first hollow needle, and a secondhollow needle. Still further embodiments include a catheter assemblyhaving a body and a hollow lumen, the catheter body being adapted andconfigured for attachment to the intravenous tubing. The catheter bodyincludes a one-way valve that prevents flow of blood through the lumenwhen the first needle is separated from the lumen.

Another aspect of the present invention pertains to an apparatus forcollecting blood in a container and connecting to intravenous tubing.Some embodiments include a main body defining an interior including acollection cavity. Other embodiments include a first retractable needlehaving a first sharp tip, the first needle being movable from a firstextended position in which the first sharp tip is exterior to the mainbody for insertion into a blood vessel to a second retracted position inwhich the first sharp tip is within the interior. Yet other embodimentsinclude a second needle having a second sharp tip extending into thecollection cavity. Still further embodiments include a catheter assemblyhaving a body defining a hollow lumen, the catheter body being adaptedand configured for attachment to the intravenous tubing. The firstneedle and the main body are readily separable from the catheterassembly, the first needle automatically withdrawing to the secondposition after separating the first needle from the catheter assembly.

Yet another aspect of the present invention pertains to a method forobtaining a sample of blood in a container from the circulatory systemof a biological unit. Some embodiments include providing a hand-helddevice defining an interior including a collection cavity and includingfirst and second hollow needles in fluid communication with each other,and a catheter surrounding the first needle. Yet other embodimentsinclude inserting the first needle and the surrounding catheter into thecirculatory system. Still other embodiments include placing thecontainer in the collection cavity and inserting the second needle intothe container, either before or after inserting the first needle intothe circulatory system. Other embodiments include establishing fluidcommunication from the first needle to the container, separating thefirst needle and the catheter; and automatically withdrawing the firstneedle into the interior by the separating.

It will be appreciated that the various apparatus and methods describedin this summary section, as well as elsewhere in this application, canbe expressed as a large number of different combinations andsubcombinations. All such useful, novel, and inventive combinations andsubcombinations are contemplated herein, it being recognized that theexplicit expression of each of these combinations is unnecessary.

BRIEF DESCRIPTION OF THE DRAWINGS

Some of the figures shown herein may include dimensions. Further, someof the figures shown herein may have been created from scaled drawingsor from photographs that are scalable. It is understood that suchdimensions, or the relative scaling within a figure, are by way ofexample, and not to be construed as limiting.

FIG. 1 is a perspective, exploded line drawing of an apparatus accordingto one embodiment of the present invention.

FIG. 2 is a cross sectional view of the apparatus of FIG. 1, asrepresented with a drawing from a shaded CAD model, and in a first modeof operation.

FIG. 3 is a cross sectional representation of a portion of the apparatusof FIG. 2.

FIG. 4 is an enlarged cross section of a portion of the apparatus ofFIG. 2.

FIG. 5 is an enlarged cross section of a portion of the apparatus ofFIG. 2.

FIG. 6 is a cross sectional view of the apparatus of FIG. 2 in a secondmode of operation.

FIG. 7 is a cross sectional view of the apparatus of FIG. 2 in a thirdmode of operation.

FIG. 8 is a cross sectional view of the apparatus of FIG. 2 in a final,used position, and ready for disposal.

FIG. 9A shows a top plan view of an apparatus according to anotherembodiment of the present invention.

FIG. 9B shows a side elevational view of the apparatus of FIG. 9A.

FIG. 10 is a perspective, exploded line drawing of the device of FIG. 9.

FIG. 11A is a top, partially see-thru CAD representation of theembodiment of FIG. 10, assembled, and in a first mode of operation.

FIG. 11B is a side elevational cross-sectional view of the apparatus ofFIG. 11A.

FIG. 12A is a top, partially see-thru CAD representation of theembodiment of FIG. 10, assembled, and in a second mode of operation.

FIG. 12B is a side elevational cross-sectional view of the apparatus ofFIG. 12A.

FIG. 13A is a top, partially see-thru CAD representation of a portion ofthe embodiment of FIG. 10, assembled, and in a third mode of operation.

FIG. 13B is a side elevational cross-sectional view of the apparatus ofFIG. 13A.

FIG. 14A is a top, partially see-thru CAD representation of theembodiment of FIG. 10, assembled, and in a final, used position, andready for disposal.

FIG. 14B is a side elevational cross-sectional view of the apparatus ofFIG. 14A.

FIGS. 15A, 15B, and 15C are top perspective, top plan, and crosssectional line drawings, respectively, of the luer body of FIG. 10.

FIGS. 16A and 16B are top rear and top front perspective line drawings,respectively, of the holder top of FIG. 10.

FIGS. 16C, 16D, and 16E are top plan, side elevational, and crosssectional line drawings, respectively, of the apparatus of FIG. 16A.

FIGS. 17A, 17B, and 17C are top rear, side elevational, and crosssectional line drawings, respectively, of a portion of the needleassembly of FIG. 10.

FIGS. 18A and 18B are top rear and top front perspective line drawings,respectively, of the collection adapter body of FIG. 10.

FIGS. 18C and 18D are side elevational and side cross sectional linedrawings, respectively, of the apparatus of FIG. 18A, with FIG. 18Dbeing a cross sectional representation of FIG. 18C as taken along thecenterline of FIG. 18C.

FIGS. 19A and 19B are top rear and top front perspective line drawings,respectively, of the sliding disc member of FIG. 10.

FIGS. 19C and 19D are side elevational and top plan views, respectively,of the apparatus of FIG. 19A, with FIG. 19D being the view looking downfrom line 19D-19D of FIG. 19C.

FIGS. 19E and 19F are front end and rear end views, respectively, of theapparatus of FIG. 19A.

FIGS. 20A and 20B are rear elevational and top rear perspective linedrawings, respectively, of the holder body of FIG. 10.

FIGS. 20C and 20D are side elevational and cross sectional linedrawings, respectively, of the apparatus of FIG. 20A.

FIGS. 21A and 21B are top rear and top front perspective line drawings,respectively, of an alternative to the sliding disc member of FIG. 10.

FIGS. 21C and 21D are side elevational and top plan views, respectively,of the apparatus of FIG. 21A, with FIG. 21D being the view looking downfrom line 21D-21D of FIG. 21C.

FIGS. 21E and 21F are front end and rear end views, respectively, of theapparatus of FIG. 21A.

ELEMENT NUMBERING

The following is a list of element numbers and at least one noun used todescribe that element. It is understood that none of the embodimentsdisclosed herein are limited to these nouns, and these element numberscan further include other words that would be understood by a person ofordinary skill reading and reviewing this disclosure in its entirety.

10 collection vessel 11 first position 12′ movement toward secondposition 12 second position 20 apparatus 21.1 main body 21.2 collectioncavity 22 cap 24 holder top  .1 collection valve guide  .2 collectionvalve slot 25 window 26 holder body 27 cylindrical receptaclel; wall  .1distal guide and stop; groove  .2 2^(nd) complementary feature  .3proximal guide and stop; groove  .4 pocket 28 fingers 29 collectoraperture 30 IV catheter assy 32 flexible lumen 34 luer body 35 lockingfeature 36 eyelet 37 eyelet receptacle 38 valve, 1-way or 2-way 39 valvereceptacle 40 needle assembly 42 cannula, sharp tipped 44 a adapter 45flat or flattened area; groove 46 spring  .1 spring guide  .2 ridges  .3recess 47 centerline; axis 48 tube  .1 tube guide  .2 tube port  .3 tubeport  .4 tube holder 50 collection valve assy. 51 locking tabs; guidingear 52 cannula 54 b adapter body 55 body guided member 56 sheath  .1sheath coupling 57 centerline; axis 58 filter 59 filter receptacle 60sliding disk member 61 leg 62 protrusion; 1^(st) complementary feature63 cover 64 flexible hinge member; ear 65 shoulder wings 66 cannulaaperture

DESCRIPTION OF THE PREFERRED EMBODIMENT

For the purposes of promoting an understanding of the principles of theinvention, reference will now be made to the embodiments illustrated inthe drawings and specific language will be used to describe the same. Itwill nevertheless be understood that no limitation of the scope of theinvention is thereby intended, such alterations and furthermodifications in the illustrated device, and such further applicationsof the principles of the invention as illustrated therein beingcontemplated as would normally occur to one skilled in the art to whichthe invention relates. At least one embodiment of the present inventionwill be described and shown, and this application may show and/ordescribe other embodiments of the present invention. It is understoodthat any reference to “the invention” is a reference to an embodiment ofa family of inventions, with no single embodiment including anapparatus, process, or composition that should be included in allembodiments, unless otherwise stated. Further, although there may bediscussion with regards to “advantages” provided by some embodiments ofthe present invention, it is understood that yet other embodiments maynot include those same advantages, or may include yet differentadvantages. Any advantages described herein are not to be construed aslimiting to any of the claims. The usage of words indicating preference,such as “preferably,” refers to features and aspects that are present inat least one embodiment, but which are optional for some embodiments.

The use of an N-series prefix for an element number (NXX.XX) refers toan element that is the same as the non-prefixed element (XX.XX) exceptas shown and described. As an example, an element 1020.1 would be thesame as element 20.1, except for those different features of element1020.1 shown and described. Further, common elements and common featuresof related elements may be drawn in the same manner in differentfigures, and/or use the same symbology in different figures. As such, itis not necessary to describe the features of 1020.1 and 20.1 that arethe same, since these common features are apparent to a person ofordinary skill in the related field of technology. Further, it isunderstood that the features 1020.1 and 20.1 may be backward compatible,such that a feature (NXX.XX) may include features compatible with othervarious embodiments (MXX.XX), as would be understood by those ofordinary skill in the art. This description convention also applies tothe use of prime (′), double prime (″), and triple prime (′″) suffixedelement numbers. Therefore, it is not necessary to describe the featuresof 20.1, 20.1′, 20.1″, and 20.1′″ that are the same, since these commonfeatures are apparent to persons of ordinary skill in the related fieldof technology.

Although various specific quantities (spatial dimensions, temperatures,pressures, times, force, resistance, current, voltage, concentrations,wavelengths, frequencies, heat transfer coefficients, dimensionlessparameters, etc.) may be stated herein, such specific quantities arepresented as examples only, and further, unless otherwise explicitlynoted, are approximate values, and should be considered as if the word“about” prefaced each quantity. Further, with discussion pertaining to aspecific composition of matter, that description is by example only, anddoes not limit the applicability of other species of that composition,nor does it limit the applicability of other compositions unrelated tothe cited composition.

Various references may be made to one or more processes, algorithms,operational methods, or logic, accompanied by a diagram showing suchorganized in a particular sequence. It is understood that the order ofsuch a sequence is by example only, and is not intended to be limitingon any embodiment of the invention.

This document may use different words to describe the same elementnumber, or refer to an element number in a specific family of features(NXX.XX). It is understood that such multiple usage is not intended toprovide a redefinition of any term herein. It is understood that suchwords demonstrate that the particular feature can be considered invarious linguistical ways, such ways further not necessarily beingadditive or exclusive.

Various embodiments of the invention disclosed herein combine the basicelements of both an IV catheter and a blood collector and then expandsupon those features resulting in a fully automatic/passive safetyproduct that seamlessly shields the user against needle stick injuriesin one simple step. Immediately upon separation of the catheter luerfrom the main body, both cannula sharps are simultaneously andautomatically shielded within the collection holder. This renders thedevice unusable and safe for proper disposal. As used herein, the term“proximal” refers to proximity to the user, and with regards to FIG. 2or 9, to the right of the drawing. The word “distal” refers to adirection generally opposite of the proximal direction

FIG. 1 presents an exploded view of an apparatus 20 according to oneembodiment of the present invention. Apparatus 20 provides a singledevice that can be used as part of a catheter for the intravenousdelivery of medicaments, but also provide an interface through which thepatient's blood can be collected. In still further embodiments, theapparatus includes a needle that is useful for puncturing a vein of apatient, and also for providing a flow of the patient's blood into aseparate collection vessel such as a standard collection tube (notshown).

FIG. 1 shows an apparatus 20 having an IV catheter 30, needle assembly40, collection valve 50, and latching disk 60. The catheter 30, needle40, valve 50, and disk 60 are contained within a cap 22, holder top 24,and holder body 26.

Apparatus 20 can be seen in a side elevational cross sectional view inFIG. 2. The holder top 24 and holder body 26 in one embodiment aremolded plastic pieces that are joined together by any suitable process,including as examples, by way of snap fit, by adhering with a glue, byultrasonic welding, or the like. Although holder top 24 and holder body26 are shown as two separate pieces, it is understood that variousembodiments of the present invention contemplate these two componentsbeing combined into a single main body 21.1, and still furthercontemplates those other embodiments in which the various structuralfeatures of holder top 24 and holder body 26 are redistributed among twoor more different separate pieces, but which still function as a mainbody 21.1 when assembled. The catheter assembly 30, needle assembly 40,and collection valve assembly 50 are all preferably supported by theholder top 24, as will be described.

FIG. 2 shows a view of apparatus 20 in which protective cap 22 has beenremoved. It is understood that cap 22 provides for safe handling of thesterile, exposed needle 42 and catheter 32 during storage and handling.The opened proximal end of cap 22 fits over the distal-most end ofholder top 24 in a manner that provides not only for safe handling andstorage, but also for easy, ready removal by a medical professional.Preferably, cap 22 covers lumen 32 and luer 34.

Placed on the distal-most end of holder top 24 is an intravenouscatheter assembly 30. Assembly 30 includes a hollow luer body 34 thatincludes a flexible lumen 32 extending in a distal-direction. Lumen 32is preferably attached to an inner surface of luer body 34 by way of aneyelet 36. Luer body 34 also supports an internal one-way valve 38 thatis located generally in the middle of the length of body 34. In someembodiments, valve 38 is a 1-way valve, whereas in other embodiments itis a 2-way valve. Preferably, valve 38 permits cannula 42 to be extendedthrough the valve dome, without leakage. Upon withdrawal of cannula 42,the dome of valve 38 substantially seals to a fluid-tight state.

The proximal end of body 34 includes an inner diameter that establishesa friction fit over a pair of forward-extending fingers 28 that are partof holder top 24 (shown in FIG. 4). In some embodiments, luer body 34also includes a plurality of ridges on one or more outer surfaces thatassist the medical practitioner in handling of catheter assembly 30.

FIGS. 2 and 4 include cross sectional views of a needle assembly 40.Needle assembly 40 preferably includes a beveled, sharp-tipped needle 42that is fixed to the internal surfaces of a shuttling adapter 44.Cannula 42 is adapted and configured to extend within flexible lumen 32of catheter 30. The tip of cannula 42 extends beyond the end of flexiblelumen 32. During insertion of needle 42 and lumen 32 into the vein of apatient, needle 42 provides a stiffening function that maintains thecylindrical shape of lumen 32, preventing buckling of lumen 32 duringinsertion of the needle 42 and catheter 30 into the vein of the patient.

As best seen in FIG. 4, needle assembly 40 further includes a spring 46that is located between opposing, facing shoulders of adapter 44 andholder top 24. FIG. 4 shows needle assembly 40 inserted fully withincatheter assembly 30, with the resultant maximum compression of spring46. Preferably, spring 46 is a coil spring, although it is appreciatedthat various devices and methods can be used to bias apart adapter 44and the forward shoulder of holder top 24. It can also be seen in FIG. 4that cannula 42 extends through the distal-most end of valve 38, andthus provides fluid communication from the tip end aperture of needle42, to the proximal-most opened end of adapter body 44.

Referring to FIG. 4, a disk leg 61 operating as a guide for adapter 44can be seen (leg 61 preferably not being engaged with adapter 44). Afirst latching mechanism between disk 60 and holder top 24 establishesthe relative locations of needle assembly 40 and disk 60. A secondlatching mechanism establishes the relative positions of disk 60 andholder body 26. Disk 60 sits in a relaxed position between the holdertop and holder body with a slight interference fit. In a manner thatwill be described later, leg 61 of disk 60 maintains radial alignmentwithin the holder body 24 and acts as a guide to needle assembly 40 in aforwardmost position, with spring 46 under near-maximum compression,during a first mode of operation of apparatus 20.

FIG. 5 shows an enlarged sectional view of a portion of apparatus 20. Alatching disk 60 can be seen located within a generally cylindricalaperture 29 of holder body 26. Disk 60 is preferably a single, moldedpiece having a forwardly-extending leg. Various features of disk 60 areadapted and configured to provide a first latching between disk 60 andretractable need assembly 40, and a second latching between disk 60 andeither holder top 24 or holder body 26.

Collection valve assembly 50 is attached to internal support ribs ofholder top 24. Disk 60 includes a small, central aperture that looselyfits around an outer diameter of a shoulder of adapter 54. Thus, diskassembly 60 is free to move relative to adapter body 54, and body 54 isheld fixed by holder top 24. A flexible tube 48 provides fluidcommunication from adapter 44 and cannula 42 to one end of adapter body54.

Referring briefly to FIG. 2, it can be seen that adapter 54 establishesa centerline 57 generally within the center of chamber 21.2 of holderbody 26. Adapter body 44 and cannula 42 establish a second centerline 47that is generally parallel to, and offset from, centerline 57. However,it is understood that yet other embodiments of the present inventioncontemplate relative arrangements of the centerlines of needle assembly40 and collection valve assembly 50, including non-parallel arrangements(in which centerline 57 and aperture 29 of holder body 26 would beangled upward, away from the patient, referring to FIG. 2) and alsothose embodiments in which centerlines 47 and 57 are not offset (such aswhen the two axes are generally aligned).

Referring again to FIG. 5, it can be seen that adapter 54 supports acannula 52 that extends rearward toward the proximal opening 29 ofholder body 26. A conical barb at the proximal end of adapter body 54further support a flexible sheath 56 that generally surrounds and sealscannula 52 to adapter body 54. Preferably, sheath 56 is fabricated froma flexible material, such as a silicone rubber, and can therefore easilybe compressed and collapsed around cannula 52. The proximal-most end ofcannula 52 preferable includes a beveled, sharp tip for puncturing acollection vessel, as will be described later.

FIG. 5 further shows that adapter body 54 supports a porous filter 58that provides a purging function for the interior volume of cannula 42,adapter body 44, tube 48, and adapter body 54. The proximal end of disk60 includes a protrusion 62 that is shown in FIG. 6 as being heldagainst a forward ledge of holder body 26.

Apparatus 20 operates in several different modes. FIG. 1 is an explodedview of a storage mode of operation, in which catheter assembly 30 islocated at the distal-most end of holder top 24, with full compressionof spring 46. Further, in this storage mode, sheath 56 is unpunctured,and maintains the sterility of the internal flowpath of assembly 20.

FIG. 2 represents apparatus 20 in a first mode of operation. Cap 22 hasbeen removed, exposing the sharp tip of cannula 42 and the exterior offlexible lumen 32. The medical practitioner has access to hold theexterior of luer body 34, as well as the ability to hold the exterior ofholder top 24 and holder body 26. The medical practitioner places thesharp tip of cannula 40 relative to a vein of a patient, and inserts thecannula 42 and flexible lumen 32 within the vein of the patient.

In a second mode of operation, the medical practitioner can bring astandard collection vessel 10 (not shown) through aperture 29 and intothe opened proximal chamber 21.2 of holder body 26. The proximal end ofbody 26 includes a generally cylindrical chamber 21.2. The interiordimensions of the proximal end of holder body 26 are slightly greaterthan the outer diameter of the collection vessel. Therefore, thecollection vessel enters aperture 29, and the face of the collectionvessel can be brought into contact with the proximal end of sheath 56.

Preferably, the end of the collection vessel 10 is soft enough such thatthe medical practitioner can push the collection vessel against sheath56 and the sharp tip of cannula 52. By continuing to push the collectionvessel toward adapter 54, the sharp tip of cannula 52 penetrates the endof collection vessel 10, and enters the interior of the collectionvessel. However, the flexible sheath 56 does not enter the collectionvessel, and instead is compressed in buckling along cannula 52 andtoward adapter body 54.

Once the tip of cannula 52 extends within the empty volume of collectionvessel 10, fluid communication is established from the interior of thecollection vessel through cannula 52 and adapter body 54, through tube48, and into the interior flow passage of needle assembly 40. Sinceneedle assembly 40 is exposed to blood within the patient's vein, bloodcan begin to flow through needle assembly 40 and tube 48, throughcollection valve assembly 50, and into collection vessel 10.

In order to prevent any hydraulic lockup, the interior of collectionvessel 10 can be established at a pressure less than the pressure of theblood within the vein, or a suitable fluid induction device can be used.Still further, any trapped air within needle assembly 40, tube 48, andvalve assembly 50 can escape through porous filter 58. However, filter58 is preferably of a type in which the porosity of the filter ismaintained only so long as the filter does not contact blood (such as aPorex® material). Upon contact with the blood, the filter media losesporosity, such that there can be no further leakage of either trappedair or blood through the filter. As blood flows through tube 48, it canbe seen by the medical practitioner through a transparent window 25within holder top 24.

The medical practitioner maintains collection vessel 10 within holderbody 26 and in fluid communication with the vein of the patient untilsufficient blood has been collected. Multiple collection vials maybeused. After the medical professional has collected sufficient blood, thecompression is relieved and the collection vessel 10 is withdrawn. Theadapter 44 assembly still remains in a distal position, under springload, until the luer assembly 30 has separated from the Holder Top 24.The relationship between the luer body 34, holder top legs 28 andadapter 44 receiving flats 45 prevent movement. Once the user advancesthe catheter luer assembly in a distal direction beyond legs 28, thereis nothing to prevent them from flexing outward. This outward flexingreleases adapter 44 so it can move in a proximal direction, retractingtoward the proximal end of holder body 26. Needle assembly 40 can moverearward toward a receiving pocket on the end of disk 60. Both disk 60and needle assembly 40 therefore move toward the proximal end of thebody holder. The beginnings of this movement can be first seen in FIG.6. The full seating of the needle assembly in the receiving pocket ofdisk 60 can be seen in FIG. 7 Cannula 42 of needle assembly 40 retractswithin flexible lumen 32 of catheter assembly 30. However, the medicalpractitioner advances the catheter assembly 30 into the patient's vein,with the result that lumen 32 remains in fluid communication with thepatient's vein. However, as needle assembly 40 retracts, the end of theneedle assembly retracts past flexible valve 38, which acts as a one-wayvalve, and thereby closes and prevents any escape of the patient'sblood.

FIGS. 7 and 8 show the remaining retraction of needle assembly 40 withinholder body 26. As the assembly of the disk and needle retract, tube 48begins to extend. FIG. 7 shows the completed and full retraction ofneedle assembly 40 relative to disk 60. FIG. 8 shows the completed andfull retraction of the disk relative to holder 26. The aft face of disk60 is biased by spring 46 to sit against a ledge or shoulder surroundingaperture 29 of holder body 26 and locks into place preventing anyfurther movement. Tube 48 is shown in its position of maximum extensionfrom the end of adapter 44 to the end of adapter 54. The sharp tip ofcannula 42 is fully contained within holder top 24.

In some embodiments, the relationship between adapter 44 and disk 60 isgenerally for guiding disk 60 to its full proximal position. Variousembodiments do not include features that pre-stage activation uponinsertion of a collection Tube 10. The disk 60 statically stayspositioned in the holder top 24 by a simple interference fit having areverse draft. Multiple collection tubes can be used without activationsince activation (retraction of the needle assembly 40 and disk 60) doesnot occur until the catheter luer assembly 30 has separated from theholder 24.

FIGS. 9-20 pertain to an apparatus 120 according to another embodimentof the present invention. FIG. 9A and FIG. 9B show top and side externalviews, respectively, of device 120. A main body 121.1 has a protectivecap 122 on one end, and an aperture 129 defined on the opposite end, theaperture being adapted and configured to accept a collection vessel.Although what will be shown and described is an embodiment configured toaccept a vessel such as an evacuated, cylindrical vessel, the presentinvention further contemplates those embodiments in which the apertureis adapted and configured to accept any shape, size, or type ofcollection vessel, and further included those embodiments adapted andconfigured to accept tubing-like components that are in fluidcommunication with a collection reservoir.

FIG. 10 presents an exploded view of an apparatus 120 according to oneembodiment of the present invention. Apparatus 120 provides a singledevice that can be used as part of a catheter for the intravenousdelivery of medicaments, but also provide an interface through which thepatient's blood can be collected. In still further embodiments, theapparatus includes a needle that is useful for puncturing a vein of apatient, and also for providing a flow of the patient's blood into aseparate collection vessel such as a standard collection tube (notshown).

FIG. 10 shows an apparatus 120 having an IV catheter 130, needleassembly 140, collection valve 150, and latching disk 160. The catheter130, needle 140, valve 150, and disk 160 are contained within a cap 122,holder top 124, and holder body 126.

Apparatus 120 can be seen in a top elevational view in FIG. 11A and aside elevational cross sectional view (taken along the centerline ofFIG. 11A) in FIG. 11B. The holder top 124 and holder body 126 in oneembodiment are molded plastic pieces that are joined together by anysuitable process, including as examples, by way of snap fit, by adheringwith a glue, by ultrasonic welding, or the like. The catheter assembly130, needle assembly 140, and collection valve assembly 150 are allpreferably supported by the holder top 124, as will be described.

FIGS. 11A and 11B show views of apparatus 120 in which protective cap122 has been removed. It is understood that cap 122 provides for safehandling of the sterile, exposed needle 142 and catheter 132 duringstorage and handling. The opened proximal end of cap 122 fits over thedistal-most end of holder top 124 in a manner that provides not only forsafe handling and storage, but also for easy, ready removal by a medicalprofessional. Preferably, cap 122 covers lumen 132 and luer body 134,and the tip of cannula 142.

Placed on the distal-most end of holder top 124 is an intravenouscatheter assembly 130. Assembly 130 includes a hollow luer body 134 thatincludes a flexible lumen 132 extending in a distal-direction. Lumen 132is preferably attached to an inner surface of luer body 134 by way of aneyelet 136. Luer body 134 also supports an internal valve 138 within areceptacle 139 that is located generally in the middle of the length ofbody 134 (luer body 134 also being shown in FIG. 15). The proximal endof body 134 includes an inner diameter that establishes a friction fitover a pair of forward-extending fingers 128 that are part of holder top124 (also shown in FIGS. 14A and 14B). In some embodiments, luer body134 also includes a plurality of ridges on one or more outer surfacesthat assist the medical practitioner in handling of catheter assembly130. The placement of luer body 134 over fingers 128 causes the tips ofthese fingers to be pressed firmly within corresponding flats 145 ofbody 144 (as seen in FIG. 17). The inner surface of luer body 134 fitsover fingers 128 and compresses them into flats 145 so as to firmly holdneedle assembly 140 in place, and able to resist a force exerted onneedle assembly 140 by spring 146 (as will be discussed later). Luerbody 134 includes one or more locking features 135 that are adapted andconfigured for connection to another medical device.

FIG. 16 show various views of a portion of a main body according to oneembodiment of the present invention. In this embodiment, the main bodyincludes a holder top 124 that provides a variety of functions with avariety of different features. These functions and features will bedescribed, but it is understood that the present invention contemplatesthose embodiments in which one or more of these functions and featuresare not included.

Holder top 124 includes a distal end having a pair of distally extendingfingers 128 that provide for capture of needle assembly 140 as discussedherein. The proximal end of holder top 124 defines an aperture that isadapted and configured to receive therein the distal end of the holderbody 126. Further, the open proximal end of holder top 124 includes apair of distal guide/stop grooves 127.1 arranged on generally oppositesides. These grooves 127.1 coact with corresponding ears 164 of slidingdisk member 160 as will be described later. The open end of holder top124 further includes a guiding feature 127.2 that is generallycomplementary in shape to a corresponding guiding feature 162 of slidingdisk member 160, as will be discussed later.

Holder top 124 includes an outer shape adapted and configured to providea hand hold for the medical professional. As best seen in FIG. 16B,holder top 124 has a width that decreases in the distal direction, andfurther has a height that decreases in the distal direction. Thiscurving shape, which reduces from proximal to distal end, provides asecure hold of apparatus 120 within the hand and fingers of a medicalprofessional.

Holder top 124 receives within it a collection valve assembly 150, thisassembly 150 being seen in side view on FIGS. 11B, 12B, 13B, and 14B.Holder top 124 includes a guide 124.1 that receives within it acorrespondingly-shaped guided member 155 of body 154 (as seen in FIGS.18A and 18B). This guiding chamber 124.1 extends generally above needleassembly 140 and leg 161.

In apparatus 120, holder top 124 provides for the internal placement ofa needle assembly 140 and collection valve assembly 150 having cannulaaxes 147 and 157, respectively, that are generally parallel andvertically displaced from one another (as best in FIG. 11B). However,other embodiments of the present invention are not so limited. Forexample, yet other embodiments include a collection valve assemblyhaving a cannula axis that is tilted relative to the cannula axis of thefirst needle, such that the collection cavity 121.2 is tilted upward,toward the face of the user during usage. Such embodiments furthercontemplate needle assemblies 140 that retract generally into theinterior of main body 121.2, but not necessarily into the collectioncavity. Still further, although FIGS. 11A and 11B show cannula axes 147and 157 being parallel and displaced, yet other embodiments contemplatethe axes being coincident. In such embodiments, it is contemplated thatthe first and second cannulas 142 and 152 can be unitary, such that boththe needle assembly 140 and the cannula 152 retract from a first,ready-to-use position to a second, used position, after removal ofcatheter assembly 130 or actuation of some other retraction-causingfeature.

Referring to FIGS. 16C and 16E, it can be seen that holder top 124includes a slot 124.2 that is adapted and configured to receive withinit a corresponding guiding ear or locking tab 151 of adapter body 154(as best seen in FIGS. 18A and 18B). The coaction of slot 124.2 and tab151 provides for alignment of holder body 154 relative to holder top 124(and therefore alignment with needle assembly 140). Referring to FIG.18B, it can be seen that tab 151 in some embodiments provides aunidirectional, snap fit. Tab 151 has an angled, expanding leading edgeto assist in temporary expansion of guide 124.1 during assembly, yetalso includes a squared-off trailing edge that makes holder body 154resistant to accidental disassembly and removal, the outermost diametralportions of ear 151 being in interference with portions of body 124after the entire tab 151 is contained within slot 124.2, such that thetemporarily expanded holder top 124.1 snaps back into place.

FIG. 11B shows a cross sectional view of a needle assembly 140. Needleassembly 140 preferably includes a beveled, sharp-tipped needle 142 thatis fixed to the internal surfaces of a shuttling adapter 144. Cannula142 is adapted and configured to extend within flexible lumen 132 ofcatheter 130. The tip of cannula 142 extends beyond the end of flexiblelumen 132. During insertion of needle 142 and lumen 132 into the vein ofa patient, needle 142 provides a stiffening function that maintains thecylindrical shape of lumen 132, preventing buckling of lumen 132 duringinsertion of the needle 142 and catheter 130 into the vein of thepatient.

FIG. 17 show additional views of the adapter body 144 of needle assembly140. Body 144 includes a front cylindrical cavity to which cannula 142is attached, and which establishes a centerline 147 of cannula 142. Body144 further includes a plurality of ridges 146.1 that assist in aligningand guiding an end of spring 146 (as can be seen in FIG. 11B). Body 144further includes a shoulder 146.2 that receives an end 148.2 of spring146, and against which spring 146 exerts a load.

The proximal end of body 144 is adapted and configured to receive withinit an end of tube 148. FIG. 17C shows an internal cylindrical cavity148.2 that receives the end of tube 148. As tube 148 exits from body144, the tube makes a right angle turn through tube holding feature148.4. It can be seen that feature 148.4 includes a generallysemi-cylindrical shape that receives the outer diameter of the tube.However, this cylindrical shape is opened to the proximal end of body144 by a V-shaped pair of upper and lower walls. As best seen in FIG.17C, these angularly-shaped walls narrow down to a minimum distance thatis large enough to permit tube 148 to be squeezed past these wallsduring assembly, but small enough to prevent the assembled and inserted,right-angled tube from escaping the semi-cylindrical aperture. Theplacement of tube holding feature 148.4 on a side of body 144 providesfor less impedance by tube 148 on the retraction on needle assembly 140,by placing the sharpest turn radius of tube 148 held firmly within body144. Therefore, very little of the spring force is consumed by anyrequirement to make a sharp bend in tube 148 as it retracts (referringto FIGS. 13A and 14A).

As best seen in FIG. 11B, needle assembly 140 is acted upon by a spring146 that is located between the shoulder 146.2 of adapter 144 and arecess 146.3 of holder top 124 (as best seen in FIG. 16E). FIG. 4 showsneedle assembly 140 inserted fully within catheter assembly 130, withthe resultant maximum compression of spring 146. Preferably, spring 146is a coil spring, although it is appreciated that various devices andmethods can be used to bias apart adapter 144 and the forward shoulderof holder top 124. It can also be seen in FIG. 4 that cannula 142extends through the distal-most end of valve 138, and thus providesfluid communication from the tip end aperture of needle 142, to theproximal-most opened end of adapter body 144. Tube 148 continues thepath of fluid communication from adapter body 144 to adapter body 154,as will be discussed later.

Some embodiments of the present invention further include a slidingmember 160 that can provide a plurality of functions with an apparatus120. As one example, and as best seen in FIGS. 11A and 11B, slidingmember 160 includes a cover 163 that includes an aperture 166 throughwhich second needle 152 extends. Further, FIG. 11A shows that extendingdistally and on the bottom side of sliding member 160 is a leg 161 thatfits generally underneath and guides the distal end of needle assembly140. Still further, sliding member 160 includes a pair of outwardlyextending ears 164 that coact with the main body to prevent slidingmember 160 from moving distally forward from the first position 111,shown in FIGS. 11A and 11B. Sliding member 160 further defines a pocket127.4 that provides placement of needle assembly 140 in both thepartially retracted and fully retracted states (as seen in FIGS. 13B and14B, respectively). Still further, the ears 164 of sliding disk 160coact with main body 121.1 to prevent distal-direction movement of thecover 163 in the final, used configuration (as shown in FIGS. 14A and14B).

Referring to FIGS. 11B and 19D, a disk leg 161 operating as a guide foradapter 144 can be seen (leg 161 preferably not being engaged withadapter 144). A first latching mechanism between disk 160 and holder top124 establishes the relative locations of needle assembly 140 and disk160 in the first, ready to use position 111. A second latching mechanismestablishes the relative positions of disk 160 and holder body 126, inthe final, used second position 112. Disk 160 sits in a relaxed positionbetween the holder top and holder body with a slight interference fit.In a manner that will be described later, leg 161 of disk 160 maintainsradial alignment within the holder body 124 and acts as a guide toneedle assembly 140 in a forwardmost position 111, with spring 146 undernear-maximum compression, during a first mode of operation of apparatus120.

Sliding member 160 is also shown in FIG. 19. Sliding member 160 includesa disk-shaped proximal end 163 that includes within it a generallycentered aperture 166. A pair of flexibly hinged members or ears 164extends generally outward on opposing sides of member 160. A leg 161extends distally from the inner face of cover 163, and has a generallycurved shape to it as seen in FIGS. 19E and 19F. Sliding member 160further includes a semi-cylindrical wall 127 that defines therein apocket 127.4.

Flexible ears 164 coact with complementary-shaped distal and proximalguide/stop grooves 127.1 and 127.3, respectively. These guide/stopgrooves include a short length in the axial direction adapted andconfigured to receive the distal end of the ear, and provide guidance ofthe ear during sliding contact. The guide/stop grooves further include adistalmost endwall that is adapted and configured to coact with thecorresponding ears to prevent distal motion beyond a first distalmostposition (when the apparatus 120 is ready to be used) and a seconddistalmost position (after the device has been used, and the collectioncontainer withdrawn).

Distal guide/stop 127.1 can be seen in FIGS. 16A, 16B, and 16C. Proximalguide/stop 127.3 can be seen formed into holder body 126 in FIGS. 20B,20C, and 20D. Ears 164 of sliding member 160 coact with proximal grooves127.1 to limit the distalmost travel of member 160 in the first position(as can be seen in FIG. 12A). However, ears 164 are adapted andconfigured to not interfere with the sliding motion of member 160 fromthe first position toward the second position. In the fully extended andfinal position (as seen in FIG. 14A), ear 164 coacts with groove 127.3to stop movement of member 160 in a distal direction after slidingmember 160 is fully in the second position 112.

Sliding member 160 further includes a guiding feature 162 that has ashape complementary to a guiding feature 127.2, the latter being shownin FIG. 20B and FIG. 16A. Complementary-shaped features 162 and 127.2coact to guide sliding member 160 within the main body 121.1 ofapparatus 120 (as also seen in FIG. 14B). The guiding feature 162 insome embodiments fulfills a second function as a leg 161 that fits underand generally close to the bottom of adapter body 144 (as seen in FIGS.11B and 12B). The curved shape of this leg further assists in guidingadapter body 144 into pocket 127.4, as needle assembly 144 retracts fromthe first position 111 into the second (and intermediate) position 112′(as seen in FIG. 13B). It is understood that in some embodiments theneedle body-guiding function of leg 161 and the sliding member-guidingfunction (relative to main body 121.1) of guiding feature 162 can beaccomplished simultaneously with the tongue-like structure shown in FIG.19B. However, yet other embodiments contemplate configurations of thesliding member 160 in which these two guiding functions are performedseparately on a sliding member, and still further contemplate thoseembodiments in which these functions are accomplished not on the slidingmember but on other structure of the apparatus 120.

FIGS. 11 and 12 show views of a portion of apparatus 120. A latchingdisk 160 can be seen located within a generally cylindrical aperture 129of holder body 126. Disk 160 is preferably a single, molded piece havinga forwardly-extending leg. Various features of disk 160 are adapted andconfigured to provide a first latching between disk 160 and retractableneed assembly 140, and a second latching between disk 160 and eitherholder top 124 or holder body 126.

Collection valve assembly 150 is attached to internal support ribs ofholder top 124. Disk 160 includes a small, central aperture that looselyfits around an outer diameter of a shoulder of adapter 154. Thus, diskassembly 160 is free to move relative to adapter body 154, and body 154is held fixed by holder top 124. A flexible tube 148 provides fluidcommunication from adapter 144 and cannula 142 to one end of adapterbody 154.

Referring briefly to FIG. 11B, it can be seen that adapter 154establishes a centerline 157 generally within the center of chamber 121of holder body 126. Adapter body 144 and cannula 142 establish a secondcenterline 147 that is generally parallel to, and offset from,centerline 157. However, it is understood that yet other embodiments ofthe present invention contemplate relative arrangements of thecenterlines of needle assembly 140 and collection valve assembly 150,including non-parallel arrangements (in which centerline 157 andaperture 129 of holder body 126 would be angled upward, away from thepatient, referring to FIG. 2) and also those embodiments in whichcenterlines 147 and 157 are not offset (such as when the two axes aregenerally aligned).

It can be seen that adapter 154 supports a cannula 152 that extendsrearward toward the proximal opening 129 of holder body 126. A conicalbarb at the proximal end of adapter body 154 further support a flexiblesheath 156 that generally surrounds and seals cannula 152 to adapterbody 154. Preferably, sheath 156 is fabricated from a flexible material,such as a silicone rubber, and can therefore easily be compressed andcollapsed around cannula 152. The proximal-most end of cannula 152preferable includes a beveled, sharp tip for puncturing a collectionvessel, as will be described later.

Adapter body 154 supports a porous filter 158 that provides a purgingfunction for the interior volume of cannula 142, adapter body 144, tube148, and adapter body 154. The proximal end of disk 160 includes aprotrusion 162 that is shown in FIG. 6 as being held against a forwardledge of holder body 126.

FIG. 18 show various views of an adapter body 154 according to oneembodiment of the present invention. Body 154 includes a proximal endhaving a coupling feature 156.1 that is inserted into, and seals around,the open end of flexible sheath 156. Adjacent to coupling 156.1 is acylindrical collar that closely fits within aperture 166 of sliding diskmember 160. Adjacent to this centering collar is a receptacle 159 thatreceives within it filter 158. Referring to FIG. 18D, it can be seenthat receptacle 159 includes an aperture in the bottom that providesfluid communication to the flowpath extending along centerline 157, thisflowpath beginning at the tip of needle 142 and extending to the tip ofneedle 152, and further into the collection reservoir when thecollection reservoir is in place. By way of this secondary flowpath tofilter 158, any trapped air within the main flowpath can be releasedthrough the filer. Once the filer cavity fills with blood, the bloodcoacts with the filter media to block any outward flow from receptacle159. FIG. 18D also shows that the flowpath upstream of receptacle 159leads to a tube port 148.3 that receives an end of flexible tube 148.The other end of the flexible tube is received within the tube port148.2 that can be seen in FIG. 17.

Referring to FIGS. 18 and 11B, it can be seen that tube 148 extends fromport 148.3 and wraps around the distalmost nose of body 154, and issupported by one or more guiding tube guiding features 148.1. FIG. 11Bshows the tube extending between the guiding features 148.1 and flashwindow 125. Preferably, the portion of tubing proximate to flash window125 is transparent. The tube then extends aft (i.e., toward the right inFIG. 11B), around the body 154, and past the shoulder wings 165 ofsliding disk member 160 (see FIGS. 19B and 19D), and extends finally ina distal direction toward tubing guide 148.4 and into tube port 148.2 offirst needle body 144. With this forward-backward-forward again path oftube 148 in the first position, the lower portion of the tube is free toextend aft (i.e., in FIG. 14B to the right) in the second position 112,and thus not impede the retracting motion of needle assembly 140. Asbest seen in FIG. 14A, it can be seen that tube 148 in the secondposition extends generally toward one side of the centerline 147, withthe end of tube 148 being received within tube holding feature 148.4 ofadapter 144.

Apparatus 120 operates in several different modes. FIG. 10 is anexploded view of a storage mode of operation, in which catheter assembly130 is located at the distal-most end of holder top 124, with fullcompression of spring 146. Further, in this storage mode, sheath 156 isunpunctured, and maintains the sterility of the internal flowpath ofassembly 120.

FIGS. 11A and 11B represent apparatus 120 in a first mode of operation,and with sliding member 160 and needle assembly 140 in a first position111. Cap 122 has been removed, exposing the sharp tip of cannula 142 andthe exterior of flexible lumen 132. The medical practitioner has accessto hold the exterior of luer body 134, as well as the ability to holdthe exterior of holder top 124 and holder body 126. The medicalpractitioner places the sharp tip of cannula 140 relative to a vein of apatient, and inserts the cannula 142 and flexible lumen 132 within thevein of the patient.

In the first mode of operation, the medical practitioner can bring astandard collection vessel 110 (not shown) through aperture 129 and intothe opened proximal chamber 121 of holder body 126. The proximal end ofbody 126 includes a generally cylindrical chamber 121. The interiordimensions of the proximal end of holder body 126 are slightly greaterthan the outer diameter of the collection vessel. Therefore, thecollection vessel enters aperture 129, and the face of the collectionvessel can be brought into contact with the proximal end of sheath 156.

Preferably, the end of the collection vessel 110 is soft enough suchthat the medical practitioner can push the collection vessel againstsheath 156 and the sharp tip of cannula 152. By continuing to push thecollection vessel toward adapter 154, the sharp tip of cannula 152penetrates the end of collection vessel 110, and enters the interior ofthe collection vessel. However, the flexible sheath 156 does not enterthe collection vessel, and instead is compressed in buckling alongcannula 152 and toward adapter body 154.

Once the tip of cannula 152 extends within the empty volume ofcollection vessel 110, fluid communication is established from theinterior of the collection vessel through cannula 152 and adapter body154, through tube 148, and into the interior flow passage of needleassembly 140. Since needle assembly 140 is exposed to blood within thepatient's vein, blood can begin to flow through needle assembly 140 andtube 148, through collection valve assembly 150, and into collectionvessel 110.

In order to prevent any hydraulic lockup, the interior of collectionvessel 110 can be established at a pressure less than the pressure ofthe blood within the vein, or a suitable fluid induction device can beused. Still further, any trapped air within needle assembly 140, tube148, and valve assembly 150 can escape through porous filter 158.However, filter 158 is preferably of a type in which the porosity of thefilter is maintained only so long as the filter does not contact blood(such as a Porex® material). Upon contact with the blood, the filtermedia loses porosity, such that there can be no further leakage ofeither trapped air or blood through the filter. As blood flows throughtube 148, it can be seen by the medical practitioner through atransparent window 125 within holder top 124. The medical practitionermaintains collection vessel 10 within holder body 126 and in fluidcommunication with the vein of the patient until sufficient blood hasbeen collected. Multiple collection vials maybe used.

After the medical professional has collected sufficient blood, thecompression is relieved and the collection vessel 10 is withdrawn. TheAdapter 144 assembly still remains in a distal position, and underspring load, until the Luer assembly 130 has separated from the holdertop 124. The relationship between the luer body 134, Holder top Legs 128and adapter 144 receiving flats 145 prevent movement.

Once the user advances the catheter luer assembly in a distal directionbeyond legs 128, there is nothing to prevent leg 128 from flexingoutward. This outward flexing releases Adapter 144 so it can move in aproximal direction, retracting toward the proximal end of holder body126. Needle assembly 140 can move rearward toward a receiving pocket onthe end of disk 160, as seen in FIGS. 12A and 12B. Luer assembly 130 hasbeen removed from its frictional fit over the ears 128 of body 124, thusrelieving the normal force applied between the flat 145 of body 144 andthe tips of fingers 128. As shown in FIGS. 12A and 12B, with the releaseof the compression of the fingers into the grooves, needle assembly 140begins to move from the first position 111 to the second position 112.As shown in FIG. 12B, first needle adapter body 144 is free to move andbe guided by the curvature of leg 161. Both disk 160 and needle assembly140 therefore move toward the proximal end of the body holder.

The beginnings of this movement can be first seen in FIGS. 13A and 13B.Under the influence of the expanding spring 146, needle body 144 hasbeen urged into pocket 127.4 of sliding member 160 and into anintermediate second position 112′. As the proximal-most end of adapterbody 144 abuts the internal face of pocket 127.4, the spring force isfurther exerted on sliding member 160 to move it toward the right.Adapter body 144 and sliding member 160 are shown in an intermediatesecond position 112′, which is not a steady state location for theassembly as shown in FIG. 13B. In this position 112′, there is stillsufficient force being exerted by spring 146 to continue urging apartsliding member 160 and main body 121.1. The full seating of the needleassembly 140 in the receiving pocket 127.4 of disk 160 can be seen inFIG. 13B. Cannula 142 of needle assembly 140 retracts inward toward theinterior of main body 121.1. The medical practitioner advances thecatheter assembly 130 into the patient's vein, with the result thatlumen 132 remains in fluid communication with the patient's vein.However, as needle assembly 140 retracts, the end of the needle assemblyretracts past flexible valve 138, which acts as a one-way valve, andthereby closes and prevents any escape of the patient's blood fromcatheter 130.

FIGS. 14A and 14B show the remaining retraction of needle assembly 140within holder body 126 to the final, at rest second position 112. As theassembly of the disk and needle retract, tube 148 begins to extend.FIGS. 13A and 13B show the intermediate retraction of needle assembly140 relative to disk 160. FIGS. 14A and 14B show the completed and fullretraction of the sliding disk 160 relative to holder 126. The aft faceof disk 160 is biased by spring 146 to sit against a ledge or shouldersurrounding aperture 129 of holder body 126 and locks into placepreventing any further movement. Tube 148 is shown in its position ofmaximum extension from the end of adapter 144 to the end of adapter 154.The sharp tip of cannula 142 is fully contained within holder top 124.

In some embodiments, the relationship between Adapter 144 and disk 160is generally for guiding disk 160 to its full proximal position. Variousembodiments do not include features that pre-stage activation uponinsertion of a collection tube 110. The disk 60 statically stayspositioned in the holder top 124 by a simple interference fit having areverse draft. Multiple collection Tubes can be used without activationsince activation) retraction of the needle assembly 140 and disk 160)does not occur until the Catheter Luer assembly 130 has separated fromthe Holder 124.

FIG. 21 show various views of an alternative sliding disk member 260according to another embodiment of the present invention. Sliding member260 is substantially the same as sliding member 160 previouslydescribed. However, member 260 includes a cylindrical receptacle 227that extends generally along the length of leg 261. This cylindricallyshaped receptacle is open on one side (as best seen in FIGS. 21B and21E), through which an end of tube 148 can pass. Preferably, the axiallength of receptacle 227 is greater than the length of body 144 ofneedle assembly 140. Further, receptacle 227 preferably extends distallya sufficient amount so that in the first position, the distal end wallof receptacle 227 extends past the proximal end of body 144. Thissubstantially full length receptacle provides additional assurance ofproper guiding of assembly 140 in its transition from the first positionto the second position, as well as minimizing any possible buckling ofspring 148 as it expands going from the first position to the secondposition.

Various aspects of different embodiments of the present invention areexpressed in paragraphs X1, X2, X3, X4, X5, X6, X7, and X8 as follows:

X1. One aspect of the present invention pertains to an apparatus forcollecting blood in a container and connecting to intravenous tubing,comprising a collection cavity adapted and configured to receive thereinan end of a readily separable container; a first hollow needle having afirst sharp tip, said first needle being adapted and configured forinsertion of the first tip into a blood vessel; a second hollow needlehaving a second sharp tip extending into the collection cavity; and acatheter assembly having a body and a hollow lumen and receiving saidfirst needle within the lumen, the first sharp tip extending from thedistal end of the lumen, the catheter body having a proximal end adaptedand configured for attachment to the intravenous tubing, said catheterbody including a one-way valve; wherein said first needle and said mainbody are readily separable from said catheter assembly, and said one-wayvalve prevents flow of blood through the lumen when said first needle isseparated from the lumen.

X2. Another aspect of the present invention pertains to an apparatus forcollecting blood in a container and connecting to intravenous tubing,comprising a main body defining an interior adapted and configured witha readily separable container; a first retractable hollow needle havinga first sharp tip, said first needle being movable from a first extendedposition in which the first sharp tip is exterior to said main body to asecond retracted position in which the first sharp tip is within theinterior; a second hollow needle having a second sharp tip, said secondtip not extending outside of said main body; and a catheter assemblyhaving a body and a hollow lumen and receiving said first needle withinthe lumen, the catheter body having a proximal end adapted andconfigured for attachment to the intravenous tubing; wherein said firstneedle and said main body are readily separable from said catheterassembly, said first needle automatically retracting to the secondposition in response to separating said first needle from said catheterassembly.

X3. Yet another aspect of the present invention pertains to a method forobtaining a sample of blood in a container from the circulatory systemof a biological unit, comprising providing a hand-held device definingan interior including a collection cavity and including first and secondhollow needles in fluid communication with each other and a cathetersurrounding the first needle; inserting the first needle and thesurrounding catheter into the circulatory system; inserting the secondneedle into the container; establishing fluid communication from thefirst needle to the container; separating the first needle and thecatheter; and automatically retracting the first needle into theinterior after said separating.

X4. Still another aspect of the present invention pertains to anapparatus for collecting blood in a container, comprising a main bodyincluding a collection cavity adapted and configured to receive thereinan end of a separable container; a first retractable hollow needleslidable within said main body and having a first sharp tip, said firstneedle having a first extended position for insertion of the first tipinto a blood vessel and a second retracted position in which the firsttip is protected by said main body; a spring configured to urge saidfirst needle into the second position; a second hollow needle attachedto said main body and having a second sharp tip extending into thecollection cavity; and a catheter having a hollow lumen and receivingsaid first needle within the lumen when said first needle is in thefirst position.

X5. Still another aspect of the present invention pertain to anapparatus for collecting blood in a container, comprising a main bodyincluding a collection cavity adapted and configured to receive thereinan end of a separable container; a sliding member guided to slide alonga path within the collection cavity from a first position to a secondposition and including a cover defining an aperture; a first retractablehollow needle coupled to said main body and having a first sharp tip,wherein in the second position the first tip is protected within saidmain body; a second hollow needle attached to said main body and havinga second sharp tip extending through the aperture in the first positioninto the collection cavity; and a catheter having a hollow lumen andreceiving said first needle within the lumen when said first needle isin the first position; wherein said first needle is separated from saidlumen in the second position, and said cover protects the user fromaccidental contact with said second needle in the second position.

X6. Yet another aspect of the present invention pertains to an apparatusfor collecting blood in a container, comprising a main body including acollection cavity adapted and configured to receive therein an end of aseparable container; a first retractable hollow needle slidable withinsaid main body and having a first sharp tip, said first needle having afirst extended position for insertion of the first tip into a bloodvessel and a second retracted position in which the first tip isprotected within said main body; a second hollow needle fixedly attachedto said main body and having a second sharp tip extending toward thecollection cavity; and a catheter having a hollow lumen and receivingsaid first needle within the lumen when said first needle is in thefirst position; wherein said first needle is distal to said secondneedle in the first position, said first needle is separated from saidlumen in the second position, and which further comprises a first needlebody attached to said first needle, wherein in the second position saidfirst needle body is received within the collection cavity.

X7. Still another aspect of the present invention pertains to anapparatus for collecting blood in a container, comprising a main bodyincluding a collection cavity adapted and configured to receive thereinan end of a separable container; a first retractable hollow needleslidable within said main body and having a first sharp tip, said firstneedle having a first extended position for insertion of the first tipinto a blood vessel and a second retracted position in which the firsttip is protected within said main body, said first needle being orientedalong a first axis; a second hollow needle separate from said firstneedle and attached to said main body and having a second sharp tipextending into the collection cavity, said second needle being orientedalong a second axis that is non-coincident with the first axis; and acatheter having a hollow lumen and receiving said first needle withinthe lumen when said first needle is in the first position; wherein saidfirst needle is separated from said lumen in the second position.

X8. Yet another aspect of the present invention pertains to an apparatusfor collecting blood in a container, comprising a main body including acollection cavity adapted and configured to receive therein an end of aseparable container; a first retractable hollow needle slidable withinsaid main body and having a first sharp tip, said first needle having afirst extended position for insertion of the first tip into a bloodvessel and a second retracted position in which the first tip isprotected within said main body; a second hollow needle separate fromsaid first needle and having a second sharp tip extending into thecollection cavity a flexible tube providing fluid communication fromsaid first needle to said second needle in the first position; and acatheter having a hollow lumen and receiving said first needle withinthe lumen when said first needle is in the first position; wherein saidfirst needle is separated from said lumen in the second position.

Yet other embodiments pertain to any of the previous statements X1, X2,X3, X4, X5, X6, X7, or X8 which are combined with one or more of thefollowing other aspects. It is also understood that any of theaforementioned X paragraphs include listings of individual features thatcan be combined with individual features of other X paragraphs.

Which further comprises a transparent member permitting visualization ofthe flow of blood to said second needle.

Which further comprises a second body coupled to said second needle andproviding fluid communication from said first needle to said secondneedle, said second body including a gas purging valve that permits theescape of gas contained in the fluid flowpath from said first needle tosaid second needle.

Wherein said catheter body is coupled to said main body by a frictionalfit.

Wherein said first needle and said second needle are unitary.

Wherein said first needle and said second needle are non-unitary.

Which further comprises means for automatically retracting said firstneedle.

Wherein said retraction means includes a spring.

Which further comprises means for preventing automatic retraction of thefirst needle.

Wherein said preventing means includes a plurality of fingers eachreceived within a corresponding groove, said main body including one ofsaid fingers or said grooves and first needle body including the otherof said fingers or said grooves.

Wherein said preventing means includes a frictional fit between saidcatheter body and said main body.

Wherein after said separating and during said retracting the catheterremains inserted into the circulatory system.

Which further comprises blocking said retracting by said placing.

Wherein said providing includes a cover of the collection cavity, andwhich further comprises automatically locking the cover to preventaccess by the user to the second hollow needle.

Wherein said locking occurs automatically by said separating and byremoving the container from the collection cavity.

Which further comprises removing the container from the cavity aftersaid collecting.

Which further comprises collecting blood within the container after saidestablishing and before said separating.

Wherein said establishing is by puncturing the container with the secondneedle.

Wherein the device includes a pocket and said retracting is into thepocket.

Wherein said retracting is into the collection cavity.

Wherein said first needle is supported by a needle body having a ridge,said main body includes a recess, and said spring urges the ridge apartfrom the recess.

Which further comprises a cover for the collection cavity, and saidspring is configured to urge said cover to a position preventing accessto said second hollow needle.

Wherein said spring is a coil spring.

Wherein said second needle has an axis, the collection cavity has afirst length along the axis, said second needle extends into the cavityby a second length along the axis, and the second length is less thanthe first length.

Which further comprises a flexible sheath surrounding the second sharptip.

Wherein said sliding member includes a flexible outwardly extending ear,said main body includes a groove adapted and configured to receive theear therein, said ear and said groove coacting to prevent movement ofsaid sliding member relative to said main body when said first needle isin the first position.

Wherein said sliding member includes a flexible outwardly extending ear,said main body includes a groove adapted and configured to receive theear therein, said ear and said groove coacting to prevent movement ofsaid sliding member relative to said main body when said first needle isin the second position.

Wherein said sliding member includes an internal pocket, said firstneedle is received within a first needle body, and said first needlebody is coupled to said main body in said first position, and said firstneedle body is received within the pocket in the second position.

Wherein said sliding member includes a first feature having a crosssectional shape, said main body includes a second feature having a shapecomplementary to the shape of the first feature, and said first featureand said second feature coact to guide the sliding of said slidingmember along the path.

Wherein the cavity has an inner diameter and the cover has an outerdiameter substantially the same but less than the inner diameter.

Which further comprises a cover slidable within the collection cavity,said main body has a distalmost end, and said first needle is locatedbetween the distalmost end and the cover in the second position

Which further comprises a cover slidable within the collection cavityfrom a first position in which an aperture of said cover surrounds saidfirst needle, to a second position in which said cover closes thecollection cavity and prevents access to said second sharp tip.

Which further comprises a spring adapted and configured to urge apartsaid main body and said first needle body.

Wherein said first needle body applies a force from said spring to urgesaid cover to the second position.

Wherein the first axis and the second axis are parallel.

Wherein the first axis and the second axis are displaced from oneanother.

Wherein the first axis and the second axis are not parallel.

Wherein the second axis extends upward relative to the first axis.

Wherein said tube is adapted and configured to provide fluidcommunication from said first needle to said second needle in the secondposition.

Wherein said main body includes a window, and said flexible tube can beviewed through the window.

Wherein in the first position said first needle is generally distal tosaid second needle, and in the second position said first needle isgenerally adjacent to said second needle.

Wherein said first needle is received within a first needle body,wherein said sliding member includes a receptacle for receiving saidhollow needle body, said receptacle at least partially enclosing saidhollow needle body in the first position.

While the inventions have been illustrated and described in detail inthe drawings and foregoing description, the same is to be considered asillustrative and not restrictive in character, it being understood thatonly certain embodiments have been shown and described and that allchanges and modifications that come within the spirit of the inventionare desired to be protected.

What is claimed is:
 1. An apparatus for collecting blood in a separablecontainer, comprising: a main body defining an interior and including acollection cavity adapted and configured to receive therein an end of aseparable container; a sliding member guided to slide along a pathwithin the collection cavity from a first position to a second positionand including a cover defining an aperture; a first retractable hollowneedle coupled to said main body and having a first sharp tip, whereinin the first position the first sharp tip is extended for insertion intoa blood vessel and in the second position the first sharp tip isprotected within said main body; a second hollow needle attached to saidmain body and having a second sharp tip extending through the aperturein the first position into the collection cavity; and a catheter havinga hollow lumen and receiving said first retractable hollow needle withinthe hollow lumen when said first retractable hollow needle is in thefirst position; and a gas purging valve supported by said main body thatpermits the escape of gas contained in a fluid flowpath from said firstretractable hollow needle to said second hollow needle; wherein saidfirst retractable hollow needle is separated from said hollow lumen inthe second position, and said cover shields the second sharp tip of saidsecond hollow needle within the collection cavity in the secondposition, wherein the fluid flowpath from said first retractable hollowneedle to said second hollow needle is a first fluid flowpath, and saidgas purging valve releases escaped gas into the interior through asecond fluid flowpath.
 2. The apparatus of claim 1, wherein said slidingmember includes a flexible outwardly extending ear, said main bodyincludes a groove adapted and configured to receive the ear therein,said ear and said groove coacting to prevent movement of said slidingmember relative to said main body when said first retractable hollowneedle is in the first position.
 3. The apparatus of claim 1, whereinsaid sliding member includes a flexible outwardly extending ear, saidmain body includes a groove adapted and configured to receive the eartherein, said ear and said groove coacting to prevent movement of saidsliding member relative to said main body when said first retractablehollow needle is in the second position.
 4. The apparatus of claim 1,wherein said sliding member includes an internal pocket, said firstretractable hollow needle is received within a first needle body, andsaid first needle body is coupled to said main body in said firstposition, and said first needle body is received within the internalpocket in the second position.
 5. The apparatus of claim 1, wherein saidsliding member includes a first feature having a cross sectional shape,said main body includes a second feature having a shape complementary tothe shape of the first feature, and said first feature and said secondfeature coact to guide the sliding of said sliding member along thepath.
 6. The apparatus of claim 1, wherein the collection cavity has aninner diameter and the cover has an outer diameter substantially thesame as the inner diameter but less than the inner diameter.
 7. Theapparatus of claim 1, wherein said first retractable hollow needleautomatically retracts to the second position in response to separatingsaid first retractable hollow needle from said catheter, and whichfurther comprises means for automatically retracting said firstretractable hollow needle.
 8. The apparatus of claim 7, wherein saidmeans for automatically retracting includes a spring in a state ofcompression in the first position.
 9. The apparatus of claim 1, whereinsaid first retractable hollow needle automatically retracts to thesecond position in response to separating said first retractable hollowneedle from said catheter, and which further comprises means forpreventing automatic retraction of the first retractable hollow needle.10. The apparatus of claim 9, further comprising a first needle bodysupporting said first retractable hollow needle, and wherein said meansfor preventing automatic retraction includes a plurality of fingers eachreceived within a corresponding flattened area, said main body includingone of said fingers or said flattened areas and said first needle bodyincluding the other of said fingers or said flattened areas.
 11. Theapparatus of claim 9, wherein said preventing means includes africtional fit between said catheter and said main body.
 12. Theapparatus of claim 1, which further comprises a flexible tube providingfluid communication between said first retractable hollow needle andsaid second hollow needle, wherein said main body includes a window, andsaid flexible tube can be viewed through the window.
 13. The apparatusof claim 1, wherein said catheter includes a luer adapted and configuredfor attachment to intravenous tubing.
 14. The apparatus of claim 1,wherein said first retractable hollow needle and said second hollowneedle are in a fluid flowpath adapted and configured to provide bloodto the separable container.
 15. The apparatus of claim 1, wherein saidfirst retractable hollow needle is separate from said second hollowneedle.
 16. The apparatus of claim 1, which further comprises a flexibletube providing fluid communication between said first retractable hollowneedle and said second hollow needle in both the first position and thesecond position.
 17. The apparatus of claim 1, which further comprises aflexible sheath surrounding the second sharp tip.
 18. The apparatus ofclaim 1, wherein said gas purging valve is adapted and configured toblock the second fluid flowpath after contact with blood.
 19. Theapparatus of claim 1, which further comprises a spring adapted andconfigured to bias said cover to the second position, and afterseparation of said first retractable hollow needle from said hollowlumen said spring automatically urges said cover to shield said secondhollow needle within the collection cavity.
 20. The apparatus of claim19, wherein after separation of said first retractable hollow needlefrom said hollow lumen said cover shields said first retractable hollowneedle within the collection cavity.